Canonical Allele Identifier: CA348173184
Gene: GLI2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120989189G>T , CM000664.2:g.120989189G>T GRCh38
NC_000002.11:g.121746765G>T , CM000664.1:g.121746765G>T GRCh37
NC_000002.10:g.121463235G>T NCBI36
NG_009030.1:g.196899G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000361492.9:c.3224G>T MANE Select ENSP00000354586.5:p.Gly1075Val
ENST00000452319.6:c.3275G>T ENSP00000390436.1:p.Gly1092Val
ENST00000341310.10:c.*2323G>T ENSP00000344473.6:n.*2323G>T
ENST00000361492.8:c.3275G>T ENSP00000354586.4:p.Gly1092Val
ENST00000438299.5:c.*2374G>T ENSP00000400593.1:n.*2374G>T
ENST00000445186.5:c.*2374G>T ENSP00000397488.1:n.*2374G>T
ENST00000452319.5:c.3275G>T ENSP00000390436.1:p.Gly1092Val
ENST00000452692.5:c.*2323G>T ENSP00000403715.1:n.*2323G>T
NM_005270.4:c.3275G>T NP_005261.2:p.Gly1092Val
XM_006712422.1:c.3224G>T XP_006712485.1:p.Gly1075Val
XM_011510969.1:c.3257G>T XP_011509271.1:p.Gly1086Val
XM_011510970.1:c.3134G>T XP_011509272.1:p.Gly1045Val
XM_011510971.1:c.3080G>T XP_011509273.1:p.Gly1027Val
XM_011510972.1:c.3080G>T XP_011509274.1:p.Gly1027Val
XM_011510973.1:c.2900G>T XP_011509275.1:p.Gly967Val
XM_011510974.1:c.2849G>T XP_011509276.1:p.Gly950Val
XM_006712422.3:c.3224G>T XP_006712485.1:p.Gly1075Val
XM_011510969.2:c.3527G>T XP_011509271.2:p.Gly1176Val
XM_011510970.2:c.3134G>T XP_011509272.1:p.Gly1045Val
XM_011510971.2:c.3080G>T XP_011509273.1:p.Gly1027Val
XM_011510972.2:c.3176G>T XP_011509274.2:p.Gly1059Val
XM_011510973.2:c.2900G>T XP_011509275.1:p.Gly967Val
XM_011510974.2:c.2849G>T XP_011509276.1:p.Gly950Val
XM_017003818.1:c.3476G>T XP_016859307.1:p.Gly1159Val
XM_024452794.1:c.3275G>T XP_024308562.1:p.Gly1092Val
XM_024452795.1:c.3275G>T XP_024308563.1:p.Gly1092Val
NM_001371271.1:c.3275G>T NP_001358200.1:p.Gly1092Val
NM_001374353.1:c.3224G>T MANE Select NP_001361282.1:p.Gly1075Val
NM_001374354.1:c.2849G>T NP_001361283.1:p.Gly950Val
NM_005270.5:c.3275G>T NP_005261.2:p.Gly1092Val